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Items: 1 to 20 of 277

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5937716copy number variation1nstd209human GRCh38 chr16: 70,274,497-70,275,533 , GRCh37.p13 chr16: 70,308,400-70,309,436 RN7SL279P, AARS1
    nsv5936960copy number variation1nstd209human GRCh38 chr16: 70,275,391-70,275,537 , GRCh37.p13 chr16: 70,309,294-70,309,440 RN7SL279P, AARS1
    nsv5712070mobile element insertion1nstd211human GRCh38 chr16: 70,286,092-70,286,092 , GRCh37.p13 chr16: 70,319,995-70,319,995 AARS1
    nsv5669930inversion1nstd207human GRCh38 chr16: 70,123,796-74,346,113 , GRCh37.p13 chr16: 70,157,699-74,380,011 , AARS1, 83 more genes
    nsv5592874copy number variation1nstd207human GRCh38 chr16: 70,275,391-70,275,537 , GRCh37.p13 chr16: 70,309,294-70,309,440 RN7SL279P, AARS1
    nsv5557110sequence alteration1nstd206human GRCh38 chr16: 70,117,371-74,396,141 , GRCh37.p13 chr16: 70,151,274-74,430,039 , TAT, 84 more genes
    nsv5550600insertion1nstd206human GRCh38 chr16: 70,273,674-70,273,674 , GRCh37.p13 chr16: 70,307,577-70,307,577 AARS1
    nsv5525543copy number variation1nstd206human GRCh38 chr16: 70,269,330-70,269,382 , GRCh37.p13 chr16: 70,303,233-70,303,285 AARS1
    nsv5520945copy number variation1nstd206human GRCh38 chr16: 70,280,628-70,281,419 , GRCh37.p13 chr16: 70,314,531-70,315,322 AARS1
    nsv5520745copy number variation1nstd206human GRCh38 chr16: 70,247,722-70,274,323 , GRCh37.p13 chr16: 70,281,625-70,308,226 AARS1, RN7SL279P, 1 more genes
    nsv5517979copy number variation1nstd206human GRCh38 chr16: 70,273,635-70,275,481 , GRCh37.p13 chr16: 70,307,538-70,309,384 RN7SL279P, AARS1
    nsv5514040copy number variation1nstd206human GRCh38 chr16: 70,249,883-70,250,601 , GRCh37.p13 chr16: 70,283,786-70,284,504 AARS1, EXOSC6
    nsv5424130mobile element insertion1nstd206human GRCh38 chr16: 70,286,092-70,286,143 , GRCh37.p13 chr16: 70,319,995-70,320,046 AARS1
    nsv5339153translocation1nstd200human GRCh37 chr16: 70,285,843-70,285,843 , GRCh37 chr16: 46,879,852-46,879,852 , GRCh38.p12 chr16: 46,845,940-46,845,940 , GRCh38.p12 chr16: 70,251,940-70,251,940 AARS1, EXOSC6
    nsv5305426copy number variation1nstd204human GRCh37.p13 chr16: 70,309,294-70,313,111 , GRCh38.p13 chr16: 70,275,391-70,279,208 RN7SL279P, AARS1
    nsv5301752copy number variation1nstd204human GRCh38.p13 chr16: 70,261,600-70,263,536 , GRCh37.p13 chr16: 70,295,503-70,297,439 AARS1
    nsv5296966copy number variation1nstd204human GRCh38.p13 chr16: 70,274,582-70,275,613 , GRCh37.p13 chr16: 70,308,485-70,309,516 AARS1, RN7SL279P
    nsv5294235copy number variation1nstd204human GRCh38.p13 chr16: 70,273,651-70,275,783 , GRCh37.p13 chr16: 70,307,554-70,309,686 RN7SL279P, AARS1
    nsv5282911copy number variation1nstd204human GRCh38.p13 chr16: 70,181,301-70,407,500 , GRCh37.p13 chr16: 70,215,204-70,441,403 DDX19B, DDX19A, 8 more genes
    nsv5141016mobile element insertion1nstd203human GRCh38 chr16: 70,286,077-70,286,092 , GRCh37.p13 chr16: 70,319,980-70,319,995 AARS1
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